Variant #0000257685 (NC_000002.11:g.202593280G>A, NM_020919.3:c.2796C>T (ALS2))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.202593280G>A
DNA change (hg38) g.201728557G>A
Published as ALS2(NM_020919.3):c.2796C>T (p.S932=), ALS2(NM_020919.4):c.2796C>T (p.S932=)
ISCN -
DB-ID ALS2_000024 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.09548 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALS2 NM_020919.3 -/. - c.2796C>T r.(?) p.(Ser932=)


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